559 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MAESTRO TOTAL WRIST TAPERED CARPAL HEAD 7MM X 15MM STANDARD
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWN·December 29, 2016
PLATE, CARPAL SMALL
FDA Adverse Event
Other
·INTEGRA LIFESCIENCES CORPORATION (INTEGRA-OHIO)·Product code KWN·May 27, 2010
CARPAL POLY MEDIUM-STD
FDA Adverse Event
Other
·INTEGRA LIFESCIENCES CORPORATION (INTEGRA-OHIO)·Product code KWN·June 9, 2010
SIGMOID NOTCH
FDA Adverse Event
Other
·SMALL BONE INNOVATION·Product code KWN·June 1, 2007
CAPITATE STEM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWN·December 20, 2018
GRIP REST
FDA Adverse Event
BETTER HANDS GLOVE·Product code KWN·January 27, 2003
CARPAL POLY MEDIUM - STD
FDA Adverse Event
Injury
·INTEGRA LIFESCIENCES CORPORATION·Product code KWN·April 5, 2013
WRIST HEMIARTHROPLASTY SYSTEM
FDA Adverse Event
Injury
·ARTHROSURFACE, INC.·Product code KWN·July 6, 2020
SILASTIC (R) CARPAL LUNATE IMPLANT
FDA Adverse Event
Injury
·DOW CORNING CORP.·Product code KWN·May 20, 1997
UNKNOWN CARPAL BALL IMPLANT
FDA Adverse Event
Injury
·STRYKER GMBH·Product code KWN·October 9, 2020
RE-MOTION TOTAL WRIST SYSTEM IMPLANTS
FDA Adverse Event
Other
·SMALL BONE INNOVATIONS, INC.·Product code KWN·September 7, 2007
UNKNOWN MAESTRO WRIST RADIAL COMPONENT
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWN·March 1, 2017
UNKNOWN REMOTION WRIST CARPAL SCREW IMPLANT
FDA Adverse Event
Injury
·STRYKER GMBH·Product code KWN·March 8, 2019
UNKNOWN REMOTION TOTAL WRIST RADIAL IMPLANT
FDA Adverse Event
Injury
·STRYKER GMBH·Product code KWN·March 8, 2019
UNKNOWN REMOTION WRIST CARPAL IMPLANT
FDA Adverse Event
Injury
·STRYKER GMBH·Product code KWN·March 8, 2019
SILICONE LUNATE IMPLANT
FDA Adverse Event
Other
·UNKNOWN·Product code KWN·April 11, 1994
MAESTRO TC CARPALHD 7X15MM STD
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWN·January 24, 2018
RIGHT TOTAL WRIST CARPAL COMPONENT
FDA Adverse Event
Injury
·KINETIKOS MEDICAL INCORPORATED·Product code KWN·July 25, 2006
AMC WRIST
FDA Adverse Event
Injury
·HOWMEDICA INC.·Product code KWN·December 17, 1998
Prosthesis, Wrist, Carpal Lunate
FDA classification
FDA Class 2
·Prosthesis, Wrist, Carpal Lunate